EP2695735B1 - Cover film - Google Patents
Cover film Download PDFInfo
- Publication number
- EP2695735B1 EP2695735B1 EP12768281.3A EP12768281A EP2695735B1 EP 2695735 B1 EP2695735 B1 EP 2695735B1 EP 12768281 A EP12768281 A EP 12768281A EP 2695735 B1 EP2695735 B1 EP 2695735B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- layer
- cover film
- peel
- heat seal
- mass
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
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- 239000013039 cover film Substances 0.000 title claims description 98
- 239000000758 substrate Substances 0.000 claims description 38
- 239000004925 Acrylic resin Substances 0.000 claims description 35
- 229920000178 Acrylic resin Polymers 0.000 claims description 35
- 229920005989 resin Polymers 0.000 claims description 33
- 239000011347 resin Substances 0.000 claims description 33
- 239000004711 α-olefin Substances 0.000 claims description 31
- 239000011342 resin composition Substances 0.000 claims description 29
- 229920005604 random copolymer Polymers 0.000 claims description 22
- 230000009477 glass transition Effects 0.000 claims description 19
- 239000002216 antistatic agent Substances 0.000 claims description 17
- 229920001400 block copolymer Polymers 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- 238000001035 drying Methods 0.000 claims description 11
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 8
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 7
- 229910001887 tin oxide Inorganic materials 0.000 claims description 7
- 125000002091 cationic group Chemical group 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 239000011859 microparticle Substances 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- SOLUNJPVPZJLOM-UHFFFAOYSA-N trizinc;distiborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-][Sb]([O-])([O-])=O.[O-][Sb]([O-])([O-])=O SOLUNJPVPZJLOM-UHFFFAOYSA-N 0.000 claims description 4
- 239000011787 zinc oxide Substances 0.000 claims description 4
- 229920001890 Novodur Polymers 0.000 claims description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 227
- 238000007789 sealing Methods 0.000 description 60
- 239000010408 film Substances 0.000 description 33
- -1 polyethylene terephthalate Polymers 0.000 description 25
- 239000004793 Polystyrene Substances 0.000 description 23
- 229920002223 polystyrene Polymers 0.000 description 20
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 19
- 229920000092 linear low density polyethylene Polymers 0.000 description 19
- 239000004707 linear low-density polyethylene Substances 0.000 description 17
- 239000004698 Polyethylene Substances 0.000 description 15
- 239000011248 coating agent Substances 0.000 description 15
- 229920000573 polyethylene Polymers 0.000 description 15
- 239000000463 material Substances 0.000 description 11
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- 239000000126 substance Substances 0.000 description 11
- 229920000728 polyester Polymers 0.000 description 10
- 229920003048 styrene butadiene rubber Polymers 0.000 description 10
- 239000000839 emulsion Substances 0.000 description 9
- 239000011231 conductive filler Substances 0.000 description 8
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- 239000012298 atmosphere Substances 0.000 description 7
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- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 description 6
- 239000005020 polyethylene terephthalate Substances 0.000 description 6
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- 238000000576 coating method Methods 0.000 description 5
- 238000003851 corona treatment Methods 0.000 description 5
- 229920001684 low density polyethylene Polymers 0.000 description 5
- 239000004702 low-density polyethylene Substances 0.000 description 5
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
- 239000003990 capacitor Substances 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 229920005669 high impact polystyrene Polymers 0.000 description 4
- 239000004797 high-impact polystyrene Substances 0.000 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- 229920006267 polyester film Polymers 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
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- KWKAKUADMBZCLK-UHFFFAOYSA-N methyl heptene Natural products CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 3
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- 150000005673 monoalkenes Chemical class 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 229920002873 Polyethylenimine Polymers 0.000 description 2
- 125000005396 acrylic acid ester group Chemical group 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical class 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- WHLPIOPUASGRQN-UHFFFAOYSA-N butyl 2-methylprop-2-enoate;methyl 2-methylprop-2-enoate Chemical compound COC(=O)C(C)=C.CCCCOC(=O)C(C)=C WHLPIOPUASGRQN-UHFFFAOYSA-N 0.000 description 2
- AHVOFPQVUVXHNL-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate Chemical compound COC(=O)C(C)=C.CCCCOC(=O)C=C AHVOFPQVUVXHNL-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 229920005668 polycarbonate resin Polymers 0.000 description 2
- 239000004431 polycarbonate resin Substances 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 239000013558 reference substance Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
- XTVRLCUJHGUXCP-UHFFFAOYSA-N 3-methyleneheptane Chemical compound CCCCC(=C)CC XTVRLCUJHGUXCP-UHFFFAOYSA-N 0.000 description 1
- LDTAOIUHUHHCMU-UHFFFAOYSA-N 3-methylpent-1-ene Chemical compound CCC(C)C=C LDTAOIUHUHHCMU-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229940006460 bromide ion Drugs 0.000 description 1
- DFYKHEXCUQCPEB-UHFFFAOYSA-N butyl 2-methylprop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CCCCOC(=O)C(C)=C DFYKHEXCUQCPEB-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- QOOHYDWLGMRJNH-UHFFFAOYSA-N butyl prop-2-enoate;cyclohexyl 2-methylprop-2-enoate;methyl 2-methylprop-2-enoate Chemical compound COC(=O)C(C)=C.CCCCOC(=O)C=C.CC(=C)C(=O)OC1CCCCC1 QOOHYDWLGMRJNH-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000002041 carbon nanotube Substances 0.000 description 1
- 229910021393 carbon nanotube Inorganic materials 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 238000009820 dry lamination Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012968 metallocene catalyst Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 229920006146 polyetheresteramide block copolymer Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
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- 239000011970 polystyrene sulfonate Substances 0.000 description 1
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- 229920000123 polythiophene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
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- 239000004065 semiconductor Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
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- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Images
Classifications
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2270/00—Resin or rubber layer containing a blend of at least two different polymers
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2274/00—Thermoplastic elastomer material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/20—Properties of the layers or laminate having particular electrical or magnetic properties, e.g. piezoelectric
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/20—Properties of the layers or laminate having particular electrical or magnetic properties, e.g. piezoelectric
- B32B2307/202—Conductive
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/30—Properties of the layers or laminate having particular thermal properties
- B32B2307/308—Heat stability
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2439/00—Containers; Receptacles
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/256—Heavy metal or aluminum or compound thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
- Y10T428/264—Up to 3 mils
- Y10T428/265—1 mil or less
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2813—Heat or solvent activated or sealable
- Y10T428/2817—Heat sealable
- Y10T428/2826—Synthetic resin or polymer
Definitions
- the present invention relates to a cover film used in packages for electronic components.
- the electronic components used therein have also become progressively smaller and of higher performance, in addition to which the components are automatically mounted on printed circuit boards during assembly of the electronic devices.
- Surface-mounted electronic components are housed in carrier tape with pockets that are successively formed by thermoforming in accordance with the shapes of the electronic components.
- a cover film is laid as a lid material over the top surface of the carrier tape, and the ends of the cover film are continuously heat-sealed in the longitudinal direction with a heated seal bar to form packages.
- cover film materials those having a heat seal layer of thermoplastic resin laminated onto a biaxially stretched polyester film are used.
- Carrier tapes are usually made of thermoplastic resins, such as polystyrenes, polycarbonates or polyesters.
- Patent Document 1 As a means to provide high-speed sealability to the cover film, the use of a substrate layer of a suitable thickness for the purpose of increasing the thermal conductivity of the cover film at the time of heat sealing has been described (Patent Document 1). Additionally, the idea of lowering the necessary heat for heat-sealing by making the peel layer a suitable thickness has been described (Patent Document 2). However, the high-speed sealing described in these publications has a heat sealing time of 0.4 to 0.5 seconds, and adjustment of the thickness of the substrate layer or peel layer is not an adequate solution for the ultra high-speed heat sealing that is required for heat-sealing capacitors and resistors of recent years. On the other hand, the idea of raising the peel strength with respect to carrier tape even while reducing the heat sealing time by including a fibrous substance on the surface of the carrier tape bonding to the cover film has also been described (Patent Document 3).
- cover film of Patent Document 3 is used for carrier tapes composed of paper materials, and has insufficient ultra high-speed sealability with respect to carrier tapes of polystyrene, polycarbonate or polyester.
- the present invention is directed to a cover film to be used in combination with a carrier tape of polystyrene, polycarbonate, polyester or the like, with the purpose of enabling thermal bonding to such carrier tapes so as to have a sufficient peel strength even with a very short heat sealing time, with little variation in peel strength when peeling the cover film so as to prevent components from flying out from the carrier tape when peeling the cover film from the carrier tape.
- a cover film that overcomes the problems addressed by the present invention can be obtained by a cover film comprising at least a substrate layer (A), an intermediate layer (B), a peel layer (C) and a heat seal layer (D), wherein the peel layer (C) is formed from a resin composition having a specific Vicat softening temperature, and the heat seal layer (D) is formed from a resin composition having a specific glass transition temperature.
- a first embodiment of the present invention offers a cover film comprising at least, in order, a substrate layer (A), an intermediate layer (B), a peel layer (C) and a heat seal layer (D), wherein the peel layer (C) comprises a resin composition comprising a styrenic resin composition (a) having a styrene-diene block copolymer as a main component, and an ethylene- ⁇ -olefin random copolymer (b), the ethylene- ⁇ -olefin random copolymer occupying 20 to 50 mass% of the peel layer, and having a Vicat softening temperature of 55 to 80 °C; and the heat seal layer (D) comprising an acrylic resin with a glass transition temperature of 55 to 80 °C.
- the peel layer (C) comprises a resin composition comprising a styrenic resin composition (a) having a styrene-diene block copolymer as a main component, and an ethylene- ⁇ -olef
- the thickness of the substrate layer (A) after drying is preferably 12 to 20 ⁇ m
- the thickness of the intermediate layer (B) after drying is preferably 10 to 40 ⁇ m
- the thickness of the peel layer (C) after drying is preferably 5 to 20 ⁇ m
- the total thickness of the cover film after drying is preferably 45 to 65 ⁇ m.
- an embodiment of a heat seal layer (D) of the present invention is characterized in that the heat seal layer (D) comprises 100 to 700 parts by mass of conductive microparticles of one of tin oxide, zinc oxide and zinc antimonate having a mass-average particle size of 1.0 ⁇ m or less, with respect to 100 parts by mass of the resin constituting the heat seal layer (D).
- Another embodiment of the heat seal layer (D) is characterized in that the heat seal layer (D) comprises 40 to 100 parts by mass of a cationic polymer-type anti-static agent having a quaternary ammonium salt on a side chain, with respect to 100 parts by mass of the resin constituting the heat seal layer (D).
- the present invention offers a cover film to be used in combination with carrier tapes of polystyrene, polycarbonate and polyester, which can be thermally bonded to such carrier tapes in a manner such as to obtain sufficient peel strength even with a very short sealing time, thereby increasing the number of electronic components capable of being housed in the carrier tapes per unit time and reducing variations in peel strength when peeling the cover film so as to prevent components from flying out from the carrier tape when peeling the cover film.
- the cover film of the present invention comprises at least a substrate layer (A), an intermediate layer (B), a peel layer (C) and a heat seal layer (D).
- An example of an arrangement of the cover film of the present invention is shown in Fig. 1 .
- Substrate layer (A) is a layer comprising a biaxially stretched polyester or a biaxially stretched nylon, of which biaxially stretched polyethylene terephthalate (PET) and polyethylene naphthalate (PEN), biaxially stretched 6,6-nylon and 6-nylon, and biaxially stretched polypropylene are particularly preferred.
- the films for the substrate layer it is possible to use those that are commonly used, as well as those to which an anti-static agent has been applied or kneaded in as an anti-static treatment, or those that have been subjected to a corona treatment or an easy-adhesion treatment. If the substrate layer (A) is too thin, the tensile strength of the cover film itself becomes low, making it susceptible to "film rupture" when peeling the cover film. On the other hand, if too thick, the heat-sealability of the carrier tape may decrease.
- the substrate layer is thick, the bending elasticity of the cover film itself becomes high, so that when peeling the cover film, the force of separation from the carrier tape acts at areas of low peel strength, causing the peel strength to become even lower, and increasing the variations in peel strength when peeling the cover film.
- those of thickness 12 to 20 ⁇ m are preferably used.
- an intermediate layer (B) is provided on one surface of the substrate layer (A) via an adhesive layer if needed.
- the resin constituting the intermediate layer (B) may be a low-density polyethylene (hereinafter referred to as LDPE), a linear low-density polyethylene (hereinafter referred to as LLDPE) or a linear low-density polyethylene polymerized with a metallocene catalyst (hereinafter referred to as m-LLDPE), m-LLDPEs being particularly preferred for their excellent tear strength.
- LDPE low-density polyethylene
- LLDPE linear low-density polyethylene
- m-LLDPE linear low-density polyethylene polymerized with a metallocene catalyst
- the intermediate layer (B) has the effect of alleviating disparities in head pressure when the sealing heads contact the cover film while heat-sealing the cover film to the carrier tape, enabling the substrate layer and the peel layer to be bonded evenly so as to prevent variations in peel strength when peeling the cover film.
- a LDPE can be added to the m-LLDPE to improve the film forming properties.
- the above-mentioned m-LLDPE is a copolymer having, as comonomers, an ethylene and an olefin having at least 3 carbon atoms, preferably a linear, branched or aromatic nucleus-substituted ⁇ -olefin having 3 to 18 carbon atoms.
- linear mono-olefins include propylene, 1-butene, 1-pentene, 1-hexene, 1-octane, 1-nonene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene and 1-octadecene.
- examples of branched mono-olefins include 3-methyl-1-butene, 3-methyl-1-pentene, 4-methyl-1-pentene and 2-ethyl-1-hexene.
- styrenes and the like are examples of mono-olefins substituted with an aromatic nucleus.
- These comonomers can be copolymerized with ethylenes either singly or by combining two or more types. Those using 1-hexene or 1-octene as comonomers have good tensile strength and also excel in terms of cost, and are therefore preferably used.
- the thickness of the intermediate layer (B) is preferably 10 to 40 ⁇ m. If the thickness of the intermediate layer (B) is less than 10 ⁇ m, there is a risk of the bonding strength between the substrate layer (A) and the intermediate layer (B) becoming insufficient, and the effect of reducing disparities in head pressure of the sealing heads when heat-sealing cover films to carrier tape is reduced, as a result of which variations in peel strength when peeling the cover film are increased. On the other hand, at more than 40 ⁇ m, the heat of the sealing heads is less easily transmitted to the heat seal boundary between the carrier tape and the cover film when ultra high-speed heat-sealing a cover film to a carrier tape, making it difficult to obtain sufficient peel strength with the heat seal. Additionally, the bend elasticity of the cover film itself becomes high, so during the peeling of the cover film, bending of the cover film at areas of low peel strength causes forces to act toward separation from the carrier tape, further reducing the peel strength.
- the intermediate layer (B) may be composed of two or more layers depending qn the method of production of the cover film of the present invention.
- the cover film of the present invention is provided with a peel layer (C) between the intermediate layer (B) and the heat seal layer (D).
- the thermoplastic resin used in this peel layer comprise a styrenic resin composition (a) having a styrene-diene block copolymer as a main component, and an ethylene- ⁇ -olefin random copolymer (b) at a specific blending proportion, and that component (b) occupy 20 to 50 mass% of the peel layer (C).
- This peel layer (C) obtains a bonding force with the heat seal layer (D) by means of component (a), enables the bonding force to be adjusted to an appropriate value by containing the aforementioned amount of component (b), and achieves sufficient and stable peel strength between the peel layer (C) and the heat seal layer (D) when peeling the heat-sealed cover film from the carrier tape. If the amount of component (b) in the peel layer is less than 20 mass%, the adhesive force between the peel layer (C) and the heat seal layer (D) rises, increasing the variation in peel strength and changing the peel strength with the passage of time after heat sealing. On the other hand, if the amount of component (b) exceeds 50 mass%, the bonding strength between the peel layer (C) and the heat seal layer (D) becomes low, making it difficult to obtain sufficient peel strength.
- this peel layer (C) contains a resin composition having a Vicat softening temperature of 55 to 80 °C, more preferably 60 to 75 °C, according to JIS K-7206 method A120. Specifically, this Vicat softening temperature was measured by setting a measurement sample flat beneath the tip of a needle-shaped penetrator of an unweighted load rod, five minutes later, placing weights on a weight dish so that the total force on the sample is 10 N, then raising the temperature of the heating device at a heating rate of 120 °C/hr, and recording the temperature at which the tip of the penetrator penetrates 1 mm into the sample from the position at the start of the test.
- the peel layer (C) softens during heat-sealing so that the heat of the sealing heads is not easily transmitted to the boundary between the carrier tape and the cover film, and the cover film can be heat-sealed to the carrier tape in a very short sealing time.
- the peel layer When the Vicat softening temperature of the peel layer is less than 55 °C, the peel layer can soften and become fluid when heat-sealing the cover film, as a result of which the peel layer may be squeezed from the end portion of the cover film, soiling the sealing heads and causing disparities in the peel strength, as well as changing the peel strength due to the passage of time after heat-sealing.
- the Vicat softening temperature of the peel layer (C) exceeds 80 °C, sufficient peel strength cannot be obtained for ultra high-speed heat-sealing.
- the thickness of the peel layer (C) is normally 3 to 25 ⁇ m, preferably 5 to 20 ⁇ m.
- the thickness of the peel layer (C) is normally 3 to 25 ⁇ m, preferably 5 to 20 ⁇ m.
- the thickness of the peel layer (C) is less than 3 ⁇ m, sufficient peel strength may not be obtained when heat-sealing the cover film to a carrier tape.
- the thickness of the peel layer (C) exceeds 25 ⁇ m, sufficient peel strength cannot be obtained for ultra high-speed heat-sealing, there tend to be disparities in peel strength when peeling the cover film, and the costs tend to mount.
- the peel layer (C) can normally be formed by thermally melting the resin composition to constitute the peel layer in an extruder, and extruding from an inflation die or T-die.
- the cover film of the present invention has a heat seal layer (D) on the surface of a peel layer (C).
- the thermoplastic resin constituting the heat seal layer (D) is an acrylic resin having a glass transition temperature of 55 to 80 °C, more preferably 60 to 75 °C.
- Acrylic resins are materials that are generally used to constitute carrier tapes, having superior heat-sealing capability with respect to polystyrene, polycarbonate and polyester resins.
- the acrylic resins constituting the heat seal layer (D) are resins comprising at least 50 mass% of at least one type of acryl residue including acrylic acid esters such as methyl acrylate, ethyl acrylate, propyl acrylate and butyl acrylate, methacrylic acid esters such as methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate and cyclohexyl methacrylate, and may be resins obtained by copolymerizing two or more types thereof.
- the glass transition temperature of the acrylic resin constituting the heat seal layer (D) is less than 55 °C, the change in peel strength is large when let stand for a long time after heat-sealing to a carrier tape, so the peel strength lacks stability.
- the glass transition temperature of the acrylic resin constituting the heat seal layer (D) exceeds 80 °C, sufficient peel strength cannot be obtained in the ultra high-speed heat-seal.
- the glass transition temperature is the value obtained when the heating speed is set to 10 °C per minute in the measurement method of JIS K7121.
- the glass transition temperature was measured using a thermal analyzer by setting about 1.5 mg of alumina as a reference substance and about 1.5 mg of a measured sample in the holder portion, raising the temperature of the nitrogen atmosphere from room temperature to 150 °C at a temperature ramp rate of 10 °C per minute, and measuring the difference in heat between the reference substance and the measured sample.
- a heat seal layer comprising an acrylic resin with a specific glass transition temperature is formed on the surface of a peel layer comprising a thermoplastic resin with a Vicat softening temperature of 55 to 80 °C comprising a styrene resin composition (a) and an ethylene- ⁇ -olefin random copolymer (b), thereby softening the peel layer (C) when heat-sealing so that the heat from the sealing heads can be easily transmitted to the heat seal layer, and enabling the heat seal layer to easily follow the contours of the carrier tape surface, thereby resulting in better ultra high-speed heat-sealing ability than various types of carrier tape materials such as polystyrene, polycarbonate and polyester resins which are materials constituting carrier tapes.
- the thickness of the heat seal layer (D) is normally 0.1 to 2.0 ⁇ m, preferably 0.3 to 1.0 ⁇ m.
- the thickness of the heat seal layer (D) is less than 0.1 ⁇ m, there may be insufficient anti-static properties or peel strength when the cover film is heat-sealed to carrier tape.
- the thickness of the heat seal layer (D) exceeds 2.0 ⁇ m, there is a risk of variations occurring in the peel strength when peeling the cover film, inviting cost increases.
- the heat seal layer (D) is usually formed by methods such as applying a solution in which the resin composition constituting the heat seal layer is dissolved in toluene or ethyl acetate, or applying an emulsion of the resin constituting the heat seal layer, but in the case of an application method, the thickness referred to here is the thickness after drying.
- the heat seal layer (D) may comprise at least one conductive microparticle such as tin oxide, zinc oxide or zinc antimonate.
- tin oxide doped with antimony, phosphorus or gallium raises the conductivity with little loss of transparency, and is more preferably used.
- the conductive microparticles of tin oxide, zinc oxide or zinc antimonate may be spherical or acicular. The amount added should normally be 100 to 1000 parts by mass, preferably 100 to 700 parts by mass with respect to 100 parts by mass of the thermoplastic resin constituting the heat seal layer (D).
- the heat seal layer (D) may comprise 40 to 100 parts by mass of a cationic polymeric anti-static agent having a quaternary ammonium salt side chain with monomer-derived repeating units represented by the following general formula [Chem 1] with respect to 100 parts by mass of the resin constituting the heat seal layer (D).
- a cationic polymeric anti-static agent having a quaternary ammonium salt side chain with monomer-derived repeating units represented by the following general formula [Chem 1] with respect to 100 parts by mass of the resin constituting the heat seal layer (D).
- the surface resistance of the heat seal layer (D) of the cover film will be less than 10 12 ⁇ , in which case sufficient anti-static properties cannot be provided to the cover film.
- the variation in peel strength when peeling the cover film can become too large.
- A denotes an oxygen atom or an imino group
- R 1 denotes a hydrogen atom or a methyl group
- R 2 denotes an alkylene group having 1 to 4 carbon atoms
- R 3 , R 4 and R 5 respectively denote alkyl groups having 1 to 18 carbon atoms which may be the same or different
- X- denotes an anion such as a chloride ion, a bromide ion, a sulfate ion or a methylsulfate ion
- n denotes an integer in the range of 100 to 5000.
- the method of producing the cover film is not particularly limited, and any common method may be used.
- the peel layer (C) may be pre-formed by a method such as T-die casting or inflation.
- an anchor coating agent of polyurethane, polyester, polyolefin or polyethyleneimine or the like may be applied to the surface of a substrate layer (A) such as a biaxially stretched polyester film, followed by sand lamination by extruding, from a T-die, a resin composition mainly composed of a m-LLDPE to form an intermediate layer (B) between the surface of application of the anchor coating agent and the peel layer (C), resulting in a three-layer film consisting of a substrate layer (A), an intermediate layer (B) and a peel layer (C).
- the desired cover film can be obtained by applying the resin composition constituting the heat seal layer (D) onto the surface of the peel layer (C), for example, with a gravure coater, a reverse coater, a kiss coater, an air knife coater, a Meyer bar coater or a dip coater.
- a resin composition mainly composed of a m-LLDPE constituting the intermediate layer (B) and a resin composition constituting the peel layer (C) may be separately extruded from a uniaxial extruder, then laminated by a multimanifold die to form a two-layer film consisting of an intermediate layer (B) and a peel layer (C).
- an anchor coating agent of polyurethane, polyester, polyolefin or the like is coated onto the surface, for example, of a biaxially stretched polyester film of the substrate layer (A), and the two-layer film is laminated by dry lamination onto the surface of application of the anchor coating agent, resulting in a three-layer film consisting of a substrate layer (A), an intermediate layer (B) and a peel layer (C).
- a resin composition constituting the heat seal layer (D) onto the surface of the peel layer (C) using, for example, a gravure coater, a reverse coater, a kiss coater, an air knife coater, a Meyer bar coater or a dip coater, a cover film can be obtained.
- a resin composition mainly composed of a m-LLDPE constituting a portion of intermediate layer (B) and a resin composition constituting the peel layer (C) may be separately extruded from a uniaxial extruder, then laminated with a multimanifold die to form a two-layer film consisting of parts of the intermediate layer (B) and a peel layer (C).
- an anchor coating agent of polyurethane, polyester, polyolefin, polyethyleneimine or the like is coated onto the surface, for example, of a biaxially stretched polyester film of the substrate layer (A), and the resin composition mainly composed of a m-LLDPE forming a portion of the intermediate layer (B) is extruded from a T-die between the coating surface of the anchor coating agent and the two-layer film by sand lamination, resulting in a three-layer film consisting of a substrate layer (A), an intermediate layer (B) and a peel layer (C).
- a resin composition constituting the heat seal layer (D) may be applied to the surface of the peel layer (C), for example, by a gravure coater, a reverse coater, a kiss coater, an air knife coater, a Meyer bar coater or a dip coater, to obtain a cover film.
- the intermediate layer (B) has a two-layered structure consisting of a layer formed by coextrusion with the peel layer (C) and a layer formed by sand lamination.
- the thickness of the layer formed by sand lamination is normally in the range of 10 to 20 ⁇ m.
- the surface of the substrate layer (A) of the cover film may be subjected to an anti-static treatment as needed.
- Anti-static agents such as, for example, anionic, cationic, non-ionic or betainic surfactant-type anti-static agents or polymeric anti-static agents and conductive agents such as polystyrene sulfonate and copolymers of acrylic acid esters and quaternary ammonium acrylate may be applied by roll coaters or lip coaters using gravure rollers, or by spraying. Additionally, in order to apply these anti-static agents evenly, the film surface should preferably be subjected to a corona discharge treatment or ozone treatment, preferably a corona discharge treatment, before performing the anti-static treatment.
- Cover films are used as lid members for carrier tapes which are containers for housing electronic components.
- Carrier tapes are in the form of ribbons about 8 mm to 100 mm wide, having recesses for housing the electronic components.
- the material constituting the carrier tape is not particularly limited, but the present invention can be suitably used for polystyrene, polyester or polycarbonate carrier tapes.
- the carrier tape may be made conductive by kneading carbon black or carbon nanotubes into the resin, or provided with anti-static properties by kneading in cationic, anionic or non-ionic surfactant-type anti-static agents or permanent anti-static agents such as polyether ester amides, or by applying to the surface a coating solution having a surfactant-type anti-static agent or a conductive material such as polypyrrole or polythiophene dispersed in an organic binder.
- a packaging for housing electronic components may, for example, be obtained by placing electronic components or the like in the recesses for housing electronic components in the carrier tape, then packaging them by using sealing heads to continuously heat-seal both end portions of the cover film in the longitudinal direction using a cover film as the lid member, and winding the result onto a reel. By packaging them in this form, the electronic components or the like may be stored and transported.
- the package of the present invention can be used to house and transport various types of electronic components such as diodes, transistors, capacitors, resistors and LEDs, and it particularly enables ultra high-speed heat-sealing of electronic components with a thickness of 1 mm or less such as LEDs, transistors, diodes and resistors, thereby largely preventing the occurrence of trouble when mounting electronic components.
- the package housing the electronic components is conveyed using holes known as sprocket holes for conveying the carrier tape provided on the edge portions in the longitudinal direction of the carrier tape, while peeling the cover film a little at a time, checking for the presence, orientation and position of the electronic components and extracting them with a component mounting device, then mounting them to a substrate.
- the peel strength of the cover tape with respect to the carrier tape when subjected to ultra high-speed heat-sealing at a sealing head temperature of 160 to 210 °C, should be within the range of 0.20 to 0.70 N, preferably 0.35 to 0.60 N. For this reason, for ultra high-speed sealing at a sealing head temperature of 210 °C, a cover tape with a peel strength of at least 0.20 N and preferably at least 0.35 N may be favorably used.
- the variation in peel strength should preferably be 0.30 N or less, more preferably 0.20 N or less. Additionally, after housing the electronic components in the carrier tape and heat-sealing the cover film, it may be exposed to a high-temperature environment during transport or storage, so it is important for the peel strength to remain stable even in a high-temperature environment.
- a two-agent cured polyurethane anchor coating agent was applied using a roll coater to a biaxially stretched polyethylene terephthalate film (16 ⁇ m thick) for constituting the substrate layer, and between the coating surface and the film constituting the above-described peel layer, a melted (b-1) m-LLDPE 1 "Harmorex NH745N" (Japan Polyethylene) for constituting the intermediate layer was extruded to a thickness of 25 ⁇ m, to obtain a laminated film by extrusion lamination.
- cover films were produced using the same methods as Example 1.
- This peel layer resin composition and a mixture of 50 parts by mass of (b-2) m-LLDPE 2 "Evolue SP3010” (Prime Polymer) and 50 parts by mass of (b-3) LDPE 3 "Ube Polyethylene R500” (Ube Maruzen Polyethylene) for the first intermediate layer were extruded from separate uniaxial extruders, then extruded in layers from a multimanifold T-die to obtain a two-layer film having a peel layer and first intermediate layer with thicknesses of respectively 7 ⁇ m and 25 ⁇ m.
- a two-agent cured polyurethane anchor coating agent was applied using a roll coater to a biaxially stretched polyethylene terephthalate film (16 ⁇ m thick) for constituting the substrate layer, and between the coating surface and the surface on the first intermediate layer side of the above-described two-layer film, a melted (b-1) m-LLDPE 1 "Harmorex NH745N" (Japan Polyethylene) for constituting the second intermediate layer was extruded to a thickness of 13 ⁇ m, to obtain a laminated film by extrusion lamination.
- cover films were produced using the same methods as Example 15.
- a two-agent cured polyurethane anchor coating agent was applied using a roll coater to a biaxially stretched polyethylene terephthalate film (16 ⁇ m thick) for constituting the substrate layer, and between the coating surface and the film constituting the above-described peel layer, a melted (b-1) m-LLDPE 1 "Harmorex NH745N" (Japan Polyethylene) for constituting the intermediate layer was extruded to a thickness of 25 ⁇ m, to obtain a laminated film consisting of a substrate layer/intermediate layer/peel layer by extrusion lamination.
- Table 3 The properties of this cover film are shown in Table 3.
- a 5.5 mm wide cover film was heat-sealed to an 8 mm wide polystyrene conductive carrier tape (Denka EC-R) using two sealing heads of width 0.5 mm, sealing head length 30 mm, heat sealing temperature 210 °C, sealing pressure 3.5 kgf, feed length 4 mm, and sealing time 0.008 seconds ⁇ 7.5 seals.
- the measurement of peel strength was made after letting stand for 24 hours in an atmosphere of temperature 23 °C and relative humidity 50%, and peeling 100 mm of the cover film at a peel angle of 170° to 180° at a speed of 300 mm per minute in the same atmosphere of temperature 23 °C and relative humidity 50%. After heat sealing, the cover film did not become peeled, and a peel strength of at least 0.3 N was necessary to stably house the components.
- a 5.5 mm wide cover film was heat-sealed to an 8 mm wide polystyrene conductive carrier tape (Denka EC-R) using two sealing heads of width 0.5 mm, sealing head length 30 mm, heat sealing temperature 210 °C, sealing pressure 3.5 kgf, feed length 4 mm, and sealing time 0.008 seconds x 7.5 seals, while adjusting the heat sealing temperature so as to obtain an average peel strength of 0.40 N.
- the peeling strength variation (difference between the maximum value and the minimum value) was measured when peeling 100 mm of the cover film at a peel angle of 170° to 180° at a speed of 300 mm per minute in the same atmosphere of temperature 23 °C and relative humidity 50%. Those having a peel strength of less than 0.40 N even with a heat seal temperature of 235 °C were left unevaluated.
- the peel strength variation must be held to 0.3 N or less in order to prevent components from flying out due to the disparities in peel strength.
- the heat seal temperature was adjusted to heat-seal a polystyrene carrier tape (Denka EC-R) with an average peel strength of 0.40 N.
- the peel strength was measured under the same conditions as the above paragraph (1). Those having a peel strength of less than 0.40 N even with a heat seal temperature of 235 °C were left unevaluated. Since the variation in peel strength can be expected to increase if the peel strength becomes too large after changes over time, the increase over the value of paragraph (1) must be within 0.3 N.
- a 5.5 mm wide cover film was heat-sealed to an 8 mm wide polycarbonate conductive carrier tape (3M No. 3000) using two sealing heads of width 0.5 mm, sealing head length 30 mm, heat sealing temperature 210 °C, sealing pressure 3.5 kgf, feed length 4 mm, and sealing time 0.008 seconds ⁇ 7.5 seals.
- the measurement of peel strength was made after letting stand for 24 hours in an atmosphere of temperature 23 °C and relative humidity 50%, and peeling 100 mm of the cover film at a peel angle of 170° to 180° at a speed of 300 mm per minute in the same atmosphere of temperature 23 °C and relative humidity 50%. After heat sealing, the cover film did not become peeled, and a peel strength of at least 0.3 N was necessary to stably house components.
- Mitsubishi Chemical Hiresta UPMCP-HT 450 was used to measure the surface resistance of the surface of the heat seal layer of the cover film at an applied voltage of 100 V in an atmosphere of temperature 23 °C and relative humidity 50%, using a 70 mm surface electrode with a positive electrode diameter of 50 mm and a negative electrode diameter of 70 mm. A surface resistance of 10 12 ⁇ or less was required to provide the cover film with a sufficient anti-static property.
- the cover film of the present invention can be used not only for storage and transport of various types of electronic components such as diodes, transistors, capacitors, resistors and LEDs wherein high-speed sealing is performed, but with regard to packaging by carrier tape for housing ICs and LSIs that are susceptible to the influence of static electricity, with the potential for higher utility as the trend toward ultra-high sealing progresses.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Laminated Bodies (AREA)
- Packages (AREA)
- Packaging Frangible Articles (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011081574 | 2011-04-01 | ||
PCT/JP2012/057942 WO2012137630A1 (ja) | 2011-04-01 | 2012-03-27 | カバーフィルム |
Publications (3)
Publication Number | Publication Date |
---|---|
EP2695735A1 EP2695735A1 (en) | 2014-02-12 |
EP2695735A4 EP2695735A4 (en) | 2015-05-06 |
EP2695735B1 true EP2695735B1 (en) | 2017-12-27 |
Family
ID=46969031
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP12768281.3A Active EP2695735B1 (en) | 2011-04-01 | 2012-03-27 | Cover film |
Country Status (10)
Country | Link |
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US (1) | US20140037940A1 (zh) |
EP (1) | EP2695735B1 (zh) |
JP (1) | JP5894578B2 (zh) |
KR (1) | KR101954467B1 (zh) |
CN (1) | CN103459146B (zh) |
MY (1) | MY166772A (zh) |
PH (1) | PH12013502037B1 (zh) |
SG (1) | SG194062A1 (zh) |
TW (1) | TWI617447B (zh) |
WO (1) | WO2012137630A1 (zh) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG10201801390VA (en) * | 2013-09-02 | 2018-04-27 | Denka Company Ltd | Cover film and electronic component package |
JP6322036B2 (ja) * | 2014-04-10 | 2018-05-09 | デンカ株式会社 | カバーフィルム |
CN106608426A (zh) * | 2015-10-27 | 2017-05-03 | 戚炎思 | 一种多功能保温包装材料 |
CN106608425A (zh) * | 2015-10-27 | 2017-05-03 | 戚炎思 | 一种复合型保温、隔热包装材料 |
CN106064514A (zh) * | 2016-07-25 | 2016-11-02 | 江西美源电子材料有限公司 | 用于封装纸质载带的覆盖带 |
JP6990505B2 (ja) * | 2016-10-31 | 2022-01-12 | 昭和電工パッケージング株式会社 | 蓄電デバイス用外装材、蓄電デバイス用外装ケースおよび蓄電デバイス |
JP7261537B2 (ja) * | 2016-12-02 | 2023-04-20 | 大日本印刷株式会社 | 透明導電性カバーテープ |
JP7282478B2 (ja) * | 2017-06-15 | 2023-05-29 | 凸版印刷株式会社 | 保護層転写シート |
JP7138651B2 (ja) * | 2017-10-31 | 2022-09-16 | デンカ株式会社 | カバーフィルム |
JP7028016B2 (ja) * | 2018-03-27 | 2022-03-02 | 大日本印刷株式会社 | 透明導電性カバーテープ |
CN111319869A (zh) * | 2018-12-14 | 2020-06-23 | 科腾聚合物有限责任公司 | 用于半导体封装的热封层 |
CN109628008A (zh) * | 2018-12-29 | 2019-04-16 | 浙江洁美电子科技股份有限公司 | 一种透明盖带 |
CA3162627A1 (en) * | 2019-11-29 | 2021-06-03 | Selig Sealing Products, Inc. | Foil free tabbed seal |
CN114667218A (zh) | 2020-03-19 | 2022-06-24 | 电化株式会社 | 层叠片材、容器、载带及电子部件包装体 |
JP7182587B2 (ja) * | 2020-10-30 | 2022-12-02 | 昭和電工パッケージング株式会社 | 蓄電デバイス用外装材、蓄電デバイス用外装ケースおよび蓄電デバイス |
CN114188584B (zh) * | 2021-11-14 | 2024-05-17 | 中北大学 | 基于静电纺丝与超声喷涂制备双极膜的方法 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5358785A (en) * | 1991-05-28 | 1994-10-25 | Fuji Photo Film Co., Ltd. | Laminated film and process for producing the same |
JPH11198299A (ja) * | 1998-01-16 | 1999-07-27 | Dainippon Printing Co Ltd | 蓋 材 |
JP4055918B2 (ja) | 1998-03-27 | 2008-03-05 | 大日本印刷株式会社 | 透明導電性カバーテープ |
JP2004042958A (ja) * | 2002-07-11 | 2004-02-12 | Sumitomo Bakelite Co Ltd | 電子部品包装用カバーテープ |
JP4202685B2 (ja) * | 2002-07-16 | 2008-12-24 | 大日本印刷株式会社 | 紙キャリアテープ用カバーテープ |
JP4444814B2 (ja) | 2004-12-28 | 2010-03-31 | 信越ポリマー株式会社 | カバーテープおよび電子部品包装体 |
JP4805612B2 (ja) * | 2005-06-17 | 2011-11-02 | 電気化学工業株式会社 | カバーフィルム |
JP4939835B2 (ja) * | 2006-05-16 | 2012-05-30 | 電気化学工業株式会社 | カバーフィルム |
JP2009046132A (ja) | 2007-08-16 | 2009-03-05 | Murata Mfg Co Ltd | チップ型電子部品の収納テープおよびそれを用いたテーピング電子部品。 |
WO2010018791A1 (ja) * | 2008-08-12 | 2010-02-18 | 住友ベークライト株式会社 | 電子部品包装用カバーテープおよび電子部品包装体 |
US8828535B2 (en) * | 2008-11-12 | 2014-09-09 | Denki Kagaku Kogyo Kabushiki Kaisha | Cover tape |
-
2012
- 2012-03-27 US US14/009,281 patent/US20140037940A1/en not_active Abandoned
- 2012-03-27 JP JP2013508821A patent/JP5894578B2/ja active Active
- 2012-03-27 MY MYPI2013003524A patent/MY166772A/en unknown
- 2012-03-27 CN CN201280016992.6A patent/CN103459146B/zh active Active
- 2012-03-27 KR KR1020137028462A patent/KR101954467B1/ko active IP Right Grant
- 2012-03-27 SG SG2013073929A patent/SG194062A1/en unknown
- 2012-03-27 WO PCT/JP2012/057942 patent/WO2012137630A1/ja active Application Filing
- 2012-03-27 EP EP12768281.3A patent/EP2695735B1/en active Active
- 2012-03-29 TW TW101110963A patent/TWI617447B/zh active
-
2013
- 2013-09-30 PH PH12013502037A patent/PH12013502037B1/en unknown
Non-Patent Citations (1)
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None * |
Also Published As
Publication number | Publication date |
---|---|
EP2695735A1 (en) | 2014-02-12 |
JPWO2012137630A1 (ja) | 2014-07-28 |
KR101954467B1 (ko) | 2019-03-05 |
WO2012137630A1 (ja) | 2012-10-11 |
PH12013502037B1 (en) | 2013-12-16 |
SG194062A1 (en) | 2013-11-29 |
TW201244934A (en) | 2012-11-16 |
CN103459146A (zh) | 2013-12-18 |
KR20140030167A (ko) | 2014-03-11 |
US20140037940A1 (en) | 2014-02-06 |
EP2695735A4 (en) | 2015-05-06 |
JP5894578B2 (ja) | 2016-03-30 |
MY166772A (en) | 2018-07-23 |
TWI617447B (zh) | 2018-03-11 |
CN103459146B (zh) | 2015-12-23 |
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